Table 1.
Organism | Factor | Regulated pathways | Function and biological role | Citation | |
---|---|---|---|---|---|
Migration and invasion | Human tumor (e.g. breast, colon, oral, hepatocellular carcinoma and melanoma) cell lines | NM23-H1 |
Rho - Rac1 signaling MAPK/SAPK and PI3K/Akt pathway downregulation Gelsolin hPrune EDG2 MLC TGFβ |
Inhibition of cell motility and invasion |
[28] [75] [73] [78] [79] |
D. melanogaster | AWD | FGFR PDGFR/VEGFR | Tracheogenesis and border cell migration |
[82] [84] |
|
M. musculus | NM23-M1 | Increased incidence of lung metastases in NM23-M1 KO mice prone to develop hepatocellular carcinoma | [66] | ||
Proliferation | Human breast carcinoma cell line | NM23-H1 | Suppression of Ras-MAPK signalling through KSR | Proliferation |
[37] [104] |
C. elegans | NDK-1 | Activation of Ras-MAPK signaling through KSR | Vulval development | [99] | |
Apoptotic engulfment and phagocytosis | Human macrophages (primary cell culture) | NM23-H1 | Phagocytosis of zymosan and IgG-opsonized RBCs | [122] | |
M. musculus bone marrow-derived macrophages | NM23-M1 | Engulfment of apoptotic thymocytes | [122] | ||
C. elegans | NDK-1 | Apoptotic clearance of embryonic and germ cells |
[121] [122] |
Three main processes (cell migration and invasion, proliferation, apoptotic engulfment/phagocytosis) linked to the metastatic cascade where NM23-H1 and its homologs in model organisms play an important role. Biological functions and the molecular background are also indicated if known. Related citations are listed. See details in the text